RESUMO
Biallelic variants in DI3SL2 cause Perlman Syndrome, associated increased risk for Wilms tumor. Cutis Marmorata Telangiectatica Congenita (CMTC) is a rare congenital disorder characterized by cutaneous vascular anomalies. We report a 2-year-old boy with both Wilms tumor and CMTC. Genetic testing, prompted by his complex presentation, revealed 1 somatic mutation and 1 familial germline mutation in the DIS3L2 gene, suggesting a 2-hit causation of Wilms tumor. Separately, a single GNA11 somatic mutation was identified to explain the CMTC. We suggest that genetic testing for germline mutations associated with Wilms tumor susceptibility be considered even in cases without known family history.
Assuntos
Livedo Reticular , Telangiectasia , Tumor de Wilms , Masculino , Humanos , Pré-Escolar , Telangiectasia/genética , Telangiectasia/complicações , Telangiectasia/congênito , Livedo Reticular/complicações , Mutação , Tumor de Wilms/genética , Tumor de Wilms/complicações , Doenças Raras/complicações , Exorribonucleases/genéticaRESUMO
â¢First report of a secondary somatic glioblastoma arising from MCT-MT in a patient with underlying Li-Fraumeni syndrome.â¢The rarity of glioblastoma arising from MCT-MT warrants investigation for underlying genetic predisposition.â¢Glioblastomas arising from MCT-MT appear to exhibit wild type IDH gene status.â¢Advanced-stage glioblastoma arising from MCT-MT exhibits aggressive behavior and requires adjuvant therapy.â¢Optimal adjuvant therapy regimen for glioblastoma arising from MCT-MT remains unknown.